Microvention recalls Terumo AZUR Peripheral Coil System (REF 45-451015 etc.) due to possible missing implant coils. Affected patients should contact for remedy.
The devices may be missing the implant coil.
Microvention is recalling certain Terumo AZUR Peripheral Coil Systems because they may be missing the implant coil. This could lead to improper treatment during procedures. Patients using these devices should stop using them and contact the manufacturer.
The devices may be missing the implant coil, which is critical for proper treatment during embolization procedures. Without the coil, the device may not function correctly, potentially leading to ineffective treatment or complications.
Patients who have received the recalled Terumo AZUR Peripheral Coil System devices for embolization procedures. Those with the specific REF numbers listed are most at risk.
Check the product label for Microvention, Inc. as the manufacturer. Look for REF numbers 45-451015, 45-451020, 45-451215, 45-451220, 45-451230, 45-451520, 45-451530, 45-452020, 45-452030, 45-450410, 45-450415, 45-450405, 45-450610, 45-450615, 45-450620, 45-450815, 45-450820, or MV-AZ52030HD.
Look for the manufacturer name Microvention, Inc. and the specific REF numbers listed in the recall notice.
Reach out to Microvention, Inc. for guidance on next steps if you have the recalled device.
The recalled devices are Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil Embolization System with REF numbers 45-451015, 45-451020, 45-451215, 45-451220, 45-451230, 45-451520, 45-451530, 45-452020, 45-452030, 45-450410, 45-450415, 45-450405, 45-450610, 45-450615, 45-450620, 45-450815, 45-450820, or MV-AZ52030HD.
Check the product label for Microvention, Inc. as the manufacturer and look for the specific REF numbers listed in the recall notice.
Contact Microvention, Inc. for guidance on next steps if you have the recalled device.
We’ve drafted a message you can send Microvention to request your refund or repair — edit it as you like.
Subject: Recall Z-1223-2020 — Microvention Microvention Hello, I own a Microvention that is covered by recall Z-1223-2020 from Microvention. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
